Osseointegrated Dental Implantation, Pain, Acute
Conditions
Keywords
Naproxen sodium, Acetaminophen, Postsurgical dental pain, Prostaglandins, Interleukins
Brief summary
This double-blind pilot study will evaluate the anti-inflammatory and analgesic effects of an over-the-counter (OTC) regimen of naproxen sodium versus acetaminophen in patients receiving one or two (adjacent) dental implants. It will also confirm that naproxen sodium in the OTC dosage range is a good alternative to immediate-release opioid formulations, which are subject to misuse, abuse and diversion in this patient population.
Detailed description
Placement of dental implants is a frequently performed outpatient surgical procedure, with United States dentists currently placing implants in approximately 500,000 patients per year.This procedure has become the gold standard for replacing missing teeth due to its high level of predictability and patient acceptance, with long-term success rates greater than 95%. Thus, the number of patients opting for this procedure over dentures and fixed bridges continues to increase. In the period between 1999 and 2000 only 0.7% of the USA population had missing teeth with implants in contrast to 5.7% between 2015 and 2016 It is estimated that by 2026, if the current pace of dental implant placement continues, approximately 17% of the population will have dental implants. Dental implant surgery involves the incision of gingival tissue to expose the underlying bone, followed by the creation of a precise bony cavity where the implant will be placed using a specialized surgical drill, and lastly the screwing of the implant into bone using a specialized handpiece Thus, it is not surprising that post-surgical pain is a common sequela following dental implant surgery. Patients often experience post-surgical pain for several days after the placement of one to three dental implants, but at a pain intensity level that is generally less than that of dental impaction surgery. This post-surgical pain is inflammatory in nature; thus, NSAIDs have demonstrated efficacy and are the preferred analgesics in this patient population. Postoperative administration of intranasal ketorolac (SPRIX®) and oral acetaminophen 325 mg plus codeine 30 mg have both demonstrated efficacy. The soft tissue and bony trauma associated with dental implant surgery upregulates inflammatory mediators both locally and systemically. Elevated levels of interleukin (IL)-6, IL-8, and macrophage inflammatory protein (MIP)-1β have been observed in gingival crevicular fluid (GCF) from the implant site and the adjacent teeth one week after surgery. Prostaglandin E2 has been measured in the GCF of teeth surrounding implant sites employing similar methodology. Additionally, standard periodontal flap and bony recontouring surgery, which shares many similarities to dental implant surgery, induces an upregulation in immunoreactive prostaglandin E2 and leukotriene B4 levels at the surgical site. Dental implant surgery also increases cytokine levels in plasma, indicative of a systemic inflammatory response. Thus, in addition to being a model to study the efficacy and tolerability of OTC analgesics, dental implant surgery also appears to be an excellent model to study the anti-inflammatory properties of NSAIDs such as naproxen sodium. Therefore, the investigators propose to initiate a double-blind, pilot study to evaluate the anti-inflammatory and analgesic effects of an OTC regimen of naproxen sodium versus acetaminophen in dental implant surgery patients. Notably, the vast majority of these patients are over the age of 45, a patient demographic that is rarely captured in postsurgical dental pain studies. Compared to dental impaction surgery patients, implant surgery patients possess more comorbidities such as hypertension, hyperlipidemia and hyperglycemia Thus, while dental impaction patients are typically on few if any drugs, polypharmacy is more of the norm in dental implant surgery patients. Performing a controlled study with OTC naproxen sodium in this population will provide the opportunity to confirm that its short-term use is generally safe and effective in these older, more medically complex patients. It will also confirm that naproxen sodium in the OTC dosage range is a good alternative to immediate-release opioid formulations, which are subject to misuse, abuse and diversion in this patient population.
Interventions
440 mg by mouth immediately after completion of implant surgery followed by 220 mg 12 hours later. Then 220 mg every 8 hours for the next two days.
1000 mg by mouth immediately after the completion of implant surgery followed by 1000 mg every 6 hours for 3 days after surgery with a maximum daily dose of 3000 mg.
50 mg by mouth every 6 hours as needed for pain
Sponsors
Study design
Masking description
Administration of naproxen or acetaminophen will be masked by over-encapsulation
Intervention model description
Double blind, randomized, active-controlled, two arms
Eligibility
Inclusion criteria
* Subject requires surgical placement of one or two (adjacent) dental implants * Ability to read and sign informed consent * Males and females for 18-75 years of age * Non-smokers * Negative urine drug screen
Exclusion criteria
* Advanced periodontal disease (\>20% Clinical Attachment Loss \>20% radiographic bone loss) * History of bisphosphonate usage * Medical history or medical condition that makes any of the study medications (naproxen sodium, acetaminophen, tramadol, etc.) inappropriate treatment options including any scheduled or recent cardiac procedures (within 6 months), a history of GI ulcers, liver or kidney disease, and anticoagulant or lithium intake. * History of an allergic reaction to any pain reliever/fever reducer * Contraindication to opioid use * Positive urine drug screen for drugs of abuse unless on stable doses of a non-analgesic drug for a legitimate medical purpose * Pregnancy - A urine pregnancy test will be performed immediately before the scheduled surgery on all women of child-bearing potential * Local or systemic diseases that affects wound healing and inflammatory biomarkers (diabetes, autoimmune (rheumatoid arthritis), or inflammatory disorders - osteoarthritis is allowed). * Smokers on this pilot study because it can affect levels of inflammatory biomarkers - a urine cotinine test will be performed immediately prior to the scheduled surgery on all subjects even if participant denies smoking history * History of systemic steroid use over 2 weeks within last 2 years. * Poor oral hygiene on a non-compliant individual.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Pain Intensity Scores on Numeric Pain Intensity Scale 0-6 Hours | Up to 6 hours | Median maximum pain intensity scores where 0 = no pain and 10 = worst possible pain |
| Pain Intensity Scores From 6 Through 72 Hours (Multi-dose Phase) | 6-72 hours Post initial Dose | Pain intensity scores where 0 = no pain and 10 = worst possible pain |
| Peak Plasma IL-6 Concentrations | 6 hours | Plasma IL-6 concentrations 6 hours after treatment measured by ELISA |
| Plasma IL-6 Change From Baseline | 6 hours post dose | Percent change in plasma IL-6 levels at 6 hours after treatment relative to baseline |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| COX-2 Activity | 6 hours post-dose | COX-2 activity was evaluated ex vivo by quantifying plasma prostaglandin (PG)E2 levels following lipopolysaccharide (LPS) stimulation in whole blood, |
| Rescue Analgesic Use | 0-6 hours | Number of patients requiring opioid rescue medication (tramadol) during inpatient phase (0-6 hours) in each treatment group |
| Peak GCF IL-8levels | 24 hours post-dose | Levels of IL-8 in gingival crevicular fluid measured at 24 hours after treatment |
| Rescue Medication Use Outpatient Phase (6-72 Hours) | 6-72 hours | Number of patients requiring opioid rescue medication during outpatient phase in both treatment groups |
| Peak GCF IL-1β Levels | 24 hours post-dose | Levels of IL-1β in gingival crevicular fluid measured at 24 hours after treatment |
| COX-1 Activity Percent of Baseline (Pre-surgery) | 6 hours post dose | Cyclooxygenase (COX)-1 activity was evaluated ex vivo by quantifying serum thromboxane B2 levels |
Countries
United States
Participant flow
Recruitment details
Subjects scheduled in University of Pennsylvania School of Dental Medicine Periodontics Clinic to receive the surgical placement of one or two dental implants.
Participants by arm
| Arm | Count |
|---|---|
| Naproxen Sodium Naproxen: 440 mg by mouth immediately after completion of implant surgery followed by 220 mg 12 hours later. Then 220 mg every 8 hours for the next two days.
Tramadol: 50 mg by mouth every 6 hours as needed for pain | 15 |
| Acetaminophen Acetaminophen: 1000 mg by mouth immediately after the completion of implant surgery followed by 1000 mg every 6 hours for 3 days after surgery with a maximum daily dose of 3000 mg.
Tramadol: 50 mg by mouth every 6 hours as needed for pain | 15 |
| Total | 30 |
Baseline characteristics
| Characteristic | Total | Acetaminophen | Naproxen Sodium |
|---|---|---|---|
| Age, Continuous | 46.2 years STANDARD_DEVIATION 14.3 | 45.5 years STANDARD_DEVIATION 14.2 | 46.8 years STANDARD_DEVIATION 14.9 |
| Body Mass Index (BMI) | 26.0 BMI (kg/m^2) STANDARD_DEVIATION 4 | 26.8 BMI (kg/m^2) STANDARD_DEVIATION 4.3 | 25.2 BMI (kg/m^2) STANDARD_DEVIATION 3.6 |
| Ethnicity (NIH/OMB) Hispanic or Latino | 2 Participants | 1 Participants | 1 Participants |
| Ethnicity (NIH/OMB) Not Hispanic or Latino | 28 Participants | 14 Participants | 14 Participants |
| Ethnicity (NIH/OMB) Unknown or Not Reported | 0 Participants | 0 Participants | 0 Participants |
| Length of Surgery | 78.4 Minutes STANDARD_DEVIATION 33.7 | 85.5 Minutes STANDARD_DEVIATION 30.6 | 71.1 Minutes STANDARD_DEVIATION 35.8 |
| Race (NIH/OMB) American Indian or Alaska Native | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Asian | 4 Participants | 2 Participants | 2 Participants |
| Race (NIH/OMB) Black or African American | 14 Participants | 10 Participants | 4 Participants |
| Race (NIH/OMB) More than one race | 1 Participants | 0 Participants | 1 Participants |
| Race (NIH/OMB) Native Hawaiian or Other Pacific Islander | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Unknown or Not Reported | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) White | 11 Participants | 3 Participants | 8 Participants |
| Sex: Female, Male Female | 18 Participants | 11 Participants | 7 Participants |
| Sex: Female, Male Male | 12 Participants | 4 Participants | 8 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk |
|---|---|---|
| deaths Total, all-cause mortality | 0 / 15 | 0 / 15 |
| other Total, other adverse events | 1 / 15 | 2 / 15 |
| serious Total, serious adverse events | 0 / 15 | 0 / 15 |
Outcome results
Pain Intensity Scores From 6 Through 72 Hours (Multi-dose Phase)
Pain intensity scores where 0 = no pain and 10 = worst possible pain
Time frame: 6-72 hours Post initial Dose
Population: Mean Pain Intensity Scores from 6-72 hours Following Around-the-Clock Dosing With Naproxen Sodium or Acetaminophen
| Arm | Measure | Value (MEAN) |
|---|---|---|
| Naproxen Sodium | Pain Intensity Scores From 6 Through 72 Hours (Multi-dose Phase) | 0.3 units on pain intensity scale |
| Acetaminophen | Pain Intensity Scores From 6 Through 72 Hours (Multi-dose Phase) | 1.7 units on pain intensity scale |
Pain Intensity Scores on Numeric Pain Intensity Scale 0-6 Hours
Median maximum pain intensity scores where 0 = no pain and 10 = worst possible pain
Time frame: Up to 6 hours
Population: Medium Greatest Pain Intensity Scores from 0-6 hours Following Dosing With Naproxen Sodium or Acetaminophen
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| Naproxen Sodium | Pain Intensity Scores on Numeric Pain Intensity Scale 0-6 Hours | 1 score on a scale |
| Acetaminophen | Pain Intensity Scores on Numeric Pain Intensity Scale 0-6 Hours | 3 score on a scale |
Peak Plasma IL-6 Concentrations
Plasma IL-6 concentrations 6 hours after treatment measured by ELISA
Time frame: 6 hours
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| Naproxen Sodium | Peak Plasma IL-6 Concentrations | 6.5 pg/ml |
| Acetaminophen | Peak Plasma IL-6 Concentrations | 12.1 pg/ml |
Plasma IL-6 Change From Baseline
Percent change in plasma IL-6 levels at 6 hours after treatment relative to baseline
Time frame: 6 hours post dose
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| Naproxen Sodium | Plasma IL-6 Change From Baseline | 276.9 percentage change from baseline |
| Acetaminophen | Plasma IL-6 Change From Baseline | 519.1 percentage change from baseline |
COX-1 Activity Percent of Baseline (Pre-surgery)
Cyclooxygenase (COX)-1 activity was evaluated ex vivo by quantifying serum thromboxane B2 levels
Time frame: 6 hours post dose
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| Naproxen Sodium | COX-1 Activity Percent of Baseline (Pre-surgery) | 3.7 percentage of baseline blood levels |
| Acetaminophen | COX-1 Activity Percent of Baseline (Pre-surgery) | 77.4 percentage of baseline blood levels |
COX-2 Activity
COX-2 activity was evaluated ex vivo by quantifying plasma prostaglandin (PG)E2 levels following lipopolysaccharide (LPS) stimulation in whole blood,
Time frame: 6 hours post-dose
Population: Patient in each group surgically receiving one or two implants
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| Naproxen Sodium | COX-2 Activity | 48.4 percentage of baseline blood levels |
| Acetaminophen | COX-2 Activity | 52.4 percentage of baseline blood levels |
Peak GCF IL-1β Levels
Levels of IL-1β in gingival crevicular fluid measured at 24 hours after treatment
Time frame: 24 hours post-dose
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| Naproxen Sodium | Peak GCF IL-1β Levels | 263 pg/ml |
| Acetaminophen | Peak GCF IL-1β Levels | 456 pg/ml |
Peak GCF IL-8levels
Levels of IL-8 in gingival crevicular fluid measured at 24 hours after treatment
Time frame: 24 hours post-dose
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| Naproxen Sodium | Peak GCF IL-8levels | 2962 pg/ml |
| Acetaminophen | Peak GCF IL-8levels | 5729 pg/ml |
Rescue Analgesic Use
Number of patients requiring opioid rescue medication (tramadol) during inpatient phase (0-6 hours) in each treatment group
Time frame: 0-6 hours
Population: Number of patients in each treatment group requiring opioid rescue medication (tramadol) during inpatient phase (0-6 hours)
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Naproxen Sodium | Rescue Analgesic Use | 0 participants |
| Acetaminophen | Rescue Analgesic Use | 3 participants |
Rescue Medication Use Outpatient Phase (6-72 Hours)
Number of patients requiring opioid rescue medication during outpatient phase in both treatment groups
Time frame: 6-72 hours
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Naproxen Sodium | Rescue Medication Use Outpatient Phase (6-72 Hours) | 2 participants |
| Acetaminophen | Rescue Medication Use Outpatient Phase (6-72 Hours) | 5 participants |